Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:12801 - mucopolysaccharidosis III


Disease Ontology Definition:A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme resulting in incomplete breakdown of the heparan sulfate sugar chain.

Synonyms: MPS IIIA - Sanfilippo syndrome A, MPS IIIB - Sanfilippo syndrome B, MPS IIIC - Sanfilippo syndrome C, MPS IIID - Sanfilippo syndrome D, Mucopolysaccharidosis, MPS-III, Mucopolysaccharidosis, MPS-III-B, N-acetyl-alpha-D-glucosaminidase deficiency, N-sulphoglucosamine sulphohydrolase deficiency, Sanfilippo syndrome A, Sanfilippo syndrome B, Sanfilippo's syndrome, heparan sulfate sulfatase deficiency, mucopolysaccharidosis type IIIA, mucopolysaccharidosis type IIIB, naglu deficiency,

Xenbase Genes : gns, hgsnat, sgsh, naglu

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018937 - mucopolysaccharidosis type 3


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): mucopolysaccharidosis (is_a)